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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASTN2, TRIM32
(T274S)
Single nucleotide variant
(missense variant +1 more)
Sarcotubular myopathy
GUncertain significance
ASTN2, TRIM32
(I291M)
Single nucleotide variant
(missense variant +1 more)
Bardet-Biedl syndrome 11
+3 more
GUncertain significance
ASTN2, TRIM32
(R299Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
ASTN2, TRIM32
(R394H)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
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